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Vartiainen E, Karjalainen S: Congenital and early-onset bilateral hearing impairment in children: The delay in detection. J Laryngol Otol 1997, 111:1018-1021. In this study from Finland, 39% of children with hearing loss were identified before 2 years of age. The study showed that high-risk behavioral screenings are insufficient, and demonstrates the need to use objective screening despite higher cost. More severe hearing loss is easier to treat if identified earlier.
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Lutman ME, Davis AC, Fortnum HM, Wood S: Field sensitivity of targeted neonatal hearing screening by transient-evoked otoacoustic emissions. Ear Hear 1997, 18:265-276. This study further investigates false positive and false negative results, where infants pass initial screening at birth, and later are determined to have hearing loss (conductive, sensorineural, mixed).
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Fowler DB, McCollister FP, Dahle AJ, Boppana S, Britt WJ, Pass RF: Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection. J Pediatr 1997, 130:624-630. Study to determine prevalence and stability of sensorineural hearing loss with asymptomatic cytomegalovirus. Results suggest that delayed-onset and progressive hearing loss can be presented by young children with asymptomatic congenital cytomegalovirus. Asymptomatic ctyomegalovirus infection is likely to be a leading cause of sensorineural hearing loss among young children.
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Haagerup A, Andersen JB, Blichfeldt S, Christensen MF: Biotinidase deficiency: two cases of very early presentation. Dev Med Child Neurol 1997, 39:832-835. Biotinase deficiency could cause severe central nervous system pathologies if undetected and untreated. Hearing loss is one component of sequella.
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Graziani LJ, Gringlas M, Baumgart S: Cerebrovascular complications and neurodevelopmental sequelae of neonatal ECMO. Clin Perinatol 1997, 24:655-675. Follow-up evaluations are essential due to the high risk of delayed onset hearing loss. Auditory brainstem response results suggesting hearing within normal limits are not predictive of later auditory status. Follow-up is recommended.
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Pennis E: The architecture of hearing. Science 1997, 278:1223-1224. This article provides insight into the advancements that can be made in our understanding of the anatomy and physiology of hearing through genetics. This article is written in terms that can be understood by professionals from many different fields and backgrounds.
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